We use cookies to make our websites more user-friendly and to continuously improve them. If you continue to use the website, you consent to the use of cookies. You can find more information in our privacy statement and our cookie guidelines.
These cookies are essential for the operation of the site and enable, for example, security-relevant functions. In addition, we can also use this type of cookie to determine whether you want to remain logged in to your profile in order to make our services available to you more quickly when you visit our website again.
In order to further improve our offer and our website, we collect anonymized data for statistics and analysis. With the help of these cookies we can, for example, determine the number of visitors and the effect of certain pages on our website and optimize our content.
We use these cookies to make it easier for you to use the site. For example, based on a previous (e.g. product search), you can conveniently access it when you visit our website again.
can obtain for you any new international publication.More details
Order the current issue now!
A cloud solution for document management. More details
online seminar S-417
702.10 EUR VAT included
590.00 EUR VAT excluded
DIN Members receive 15 % discount
For your team
Randolph Stender
NSF PROSYSTEM GmbH
Randolph Stender ist seit über 20 Jahren bei dem internationalen Beratungsunternehmen NFS PROSYSTEM GmbH als General Manager und Consultant tätig. Seine betreuten Kunden sind kleine, mittelständische und große nationale und internationale Hersteller von Medizinprodukten. Als Mitarbeiter unter anderem beim DKE, NAMed und der ISO TC210 (ISO 13485, ISO 14971 etc.) ist er seit mehr als 15 Jahren in der Normungsarbeit aktiv. Des Weiteren schult er als Referent, unter anderem beim DIN und an der NSF PROSYSTEM-Akademie, regelmäßig Medizinproduktehersteller, Pharmaunternehmen, Behörden und benannte Stellen zu einer Vielzahl von Themen in der Medizintechnik. Randolph Stender has been working for NSF for more than 20 years. He has 25+ years of experience in the medical device industry, including 20 years as a principal consultant and lead auditor for medical device companies. Mr. Stender holds a university degree in medical technology and is an active member of ISO TC 210/WG1 (ISO 13485), TC210/JWG1 (ISO 14971), TC 210/AHG 6 (PMS) and several other national and international committees and associations. He leads an international consulting team of more than 50 scientists and engineers. This team supports clients worldwide in the optimal execution of complex projects and interim management. Mr. Stender is author of the specialist book on quality management: ”Qualitätsmanagement für Hersteller von Medizinprodukten” (DIN Media GmbH), technical articles and expert reports. He is speaker and trainer for different organizations e. g. NSF’s Medical Device Academy, BVMed, TÜV Süd Academy, TÜV Rheinland Akademie, DIN Media on various regulatory topics.
